Enantioselective dearomatization reactions of heteroarenes by anion-binding organocatalysis

被引:22
作者
Aleksiev, Martin [1 ]
Mancheno, OlgaGarcia [1 ]
机构
[1] Univ Munster, Organ Chem Inst, Corrensstr 36-40, D-48149 Munster, Germany
基金
欧洲研究理事会;
关键词
NUCLEOPHILIC DEAROMATIZATION; ASYMMETRIC DEAROMATIZATION; DUAL-CATALYSIS; REARRANGEMENT; HETEROCYCLES; SILANEDIOL; QUINOLINES; PYRIDINES; STEGLICH; INDOLES;
D O I
10.1039/d2cc07101k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Catalytic asymmetric dearomatization of heteroaromatic compounds has received considerable attention in the last few years, since it allows for a fast expansion of the chemical space by converting relatively simple, flat molecules into complex, three dimensional structures with added value. Among different approaches, remarkable progress has been recently achieved by the development of organocatalytic dearomatization methods. In particular, the anion-binding catalysis technology has emerged as a potent alternative to metal catalysis, which together with the design of novel, tunable anion-receptor motifs, has provided new entries for the enantioselective dearomatization of heteroarenes through a chiral contact ion pair formation by activation of the electrophilic reaction partner. In this feature, we provide an overview of the different methodologies and advances in anion-binding catalyzed dearomatization reactions of different heteroarenes.
引用
收藏
页码:3360 / 3372
页数:13
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